High temperature attachment of organic molecules to substrates

ABSTRACT

This invention provides a new procedure for attaching molecules to semiconductor surfaces, in particular silicon. The molecules, which include, but are not limited to porphyrins and ferrocenes, have been previously shown to be attractive candidates for molecular-based information storage. The new attachment procedure is simple, can be completed in short times, requires minimal amounts of material, is compatible with diverse molecular functional groups, and in some instances affords unprecedented attachment motifs. These features greatly enhance the integration of the molecular materials into the processing steps that are needed to create hybrid molecular/semiconductor information storage devices.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. Ser. No. 10/628,868,filed on Jul. 28, 2003 now U.S. Pat. No. 6,943,054, which claims benefitof and priority to Ser. No. 60/489,992, filed on Jul. 25, 2003, both ofwhich are incorporated herein by reference in their entirety for allpurposes.

STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSOREDRESEARCH AND DEVELOPMENT

This invention was made with Government support under Grant No.MDA972-01-C-0072 awarded by the Army. The Government has certain rightsin this invention.

FIELD OF THE INVENTION

This invention pertains to the field of semiconductor fabrication. Inparticular this invention provides novel methods of coupling organicmolecules to group III, IV, and V elements (e.g., silicon, germanium,etc.), and the like.

BACKGROUND OF THE INVENTION

The fabrication of ordered molecular assemblies on conducting siliconand other surfaces is of considerable interest owing to its potentialapplications in the microelectronic industry. One goal of semiconductorfabrication is to increase the density of active elements provided on anintegrated circuit. In order to accomplish this, efforts have turned tothe use of self-assembling molecular structures as an alternative to, orin conjunction with various lithographic processes to form the activeelements used in integrated circuits.

In addition, interest has turned to the use of organic molecules to formsuch active elements (e.g., memory elements) (see, e.g., U.S. Pat. Nos.6,272,038, 6,212,093, and 6,208,553, and PCT Publication WO 01/03126)and/or to form components of certain devices (e.g., field effecttransistors, gates, sensors, transducers, etc.).

Organic molecules covalently attached to silicon are very stable due tothe strength of Si—O and Si—C bonds. A number of approaches exist toform a covalent link between silicon and organic molecules (Buriak andAllen (1998) J. Am. Chem. Soc., 120: 1339-1340; Bansal and Lewis (1998)J. Phys. Chem. 102: 1067-1070; Zhu et al. (1999) Langmuir 15: 8147-8154;Coulter et al. (2000) J. Vac. Sci. Technol. A 18: 1965-1970;Bourkherroub and Wayner (1999) J. Am. Chem. Soc. 121: 11513-11515;Cleland et al. (1995) Faraday Commun., 91: 4001-4003; Bateman et al.(1998) Angew. Chem. Int. Ed., 37: 2683-2685). These approaches includechemical, electrochemical and vapor deposition on a hydrogen-terminatedsilicon surface.

Such approaches, however, have typically involved difficult reactionconditions, have been relatively inefficient, have degraded the organicmolecule(s), and/or have resulted in the production of fairly toxicmaterials.

SUMMARY OF THE INVENTION

This Invention provides a new procedure for attaching molecules tosemiconductor surfaces, in particular silicon. The molecules includeporphyrins and ferrocenes, which have been previously shown to beattractive candidates for molecular-based information storage. The newattachment procedure is simple, can be completed in short times,requires minimal amounts of material, is compatible with diversemolecular functional groups, and in some instances affords unprecedentedattachment motifs. These features greatly enhance the integration of themolecular materials into the processing steps that are needed to createhybrid molecular/semiconductor information storage devices.

Thus, in one embodiment, this invention provides a method of covalentlycoupling an organic molecule to a surface of a Group II, III, IV, V, orVI element or to a semiconductor comprising a Group II, III, IV, V, orVI element (more preferably to a material comprising a Group III, IV, orV element or to a transition metal, transition metal oxide or nitrideand/or to an alloy comprising a transition metal or to another metal.

Thus in certain embodiments, this invention provides method of couplinga redox-active molecule to a surface where the method includes providingone or more heat-resistant organic molecules bearing an attachmentgroup; heating the molecule(s) or mixture of different molecules and/orthe surface to a temperature of at least about 100° C.; and contactingthe molecule(s) to the surface whereby the molecule(s) form a covalentlinkage to the surface. In certain embodiments, the organic molecule(s)are electrically coupled to the surface. The method can, optionally, beperformed under an inert atmosphere (e.g. Ar₂). In certain embodiments,the heating comprises heating the molecule(s) to a gas phase and thecontacting comprises contacting the gas phase to the surface. In certainembodiments, the heating comprises heating the molecule(s) and/or thesurface while the molecule is in contact with the surface. In certainembodiments, the heating comprises applying the molecule(s) to thesurface and then simultaneously or subsequently heating the molecule(s)and/or surface. The organic molecule(s) can be provided in a solvent ordry, or in gas phase, or otherwise not in a solvent.

In certain embodiments, the heating is to a temperature of at leastabout 100° C., preferably at least about 200° C., more preferably atleast about 300° C., and most preferably at least about 400° C. Heatingcan be accomplished by any convenient method, e.g. in a in a CVD device,in an MBE device, etc. In certain embodiments, the surface comprises amaterial selected from the group consisting of a Group III element, aGroup IV element, a Group V element, a semiconductor comprising a GroupIII element, a semiconductor comprising a Group IV element, asemiconductor comprising a Group V element, a transition metal, and atransition metal oxide. Certain preferred surfaces comprise one or moreof the following: tungsten, tantalum, and niobium Ga, Au, Ag, Cu, Al,Ta, Ti, Ru, Ir, Pt, Pd, Os, Mn, Hf, Zr, V, Nb, La, Y, Gd, Sr, Ba, Cs,Cr, Co, Ni, Zn, Ga, In, Cd, Rh, Re, W, Mo, and oxides, alloys, mixtures,and/or nitrides thereof. In certain embodiments, the surface comprises aGroup III, IV, or V, and/or a doped Group III, IV, or V element, e.g.silicon, germanium, doped silicon, doped germanium, and the like. Thesurface can, optionally, be a hydrogen passivated surface. In certainembodiments, the heat-resistant molecule is a redox-active moleculeselected from the group consisting of a porphyrin, a porphyrinicmacrocycle, an expanded porphyrin, a contracted porphyrin, a linearporphyrin polymer, a porphyrinic sandwich coordination complex, and aporphyrin array. Certain preferred redox-active molecules comprise aporphyrinic macrocycle substituted at a β-position or at ameso-position. Certain preferred redox-active molecules comprise aporphyrinic macrocycle containing at least two porphyrins of equalenergies held apart from each other at a spacing less than about 50 Åsuch that the molecule has an even or an odd hole oxidation where thehole hops between the two porphyrins, and where the odd hole oxidationstate is different from and distinguishable from another oxidation stateof the porphyrinic macrocycle.

In certain embodiments, the attachment group comprises an arylfunctional group and/or an alkyl attachment group. In certainembodiments, the aryl functional group comprises a functional groupselected from the group consisting of bromo, iodo, hydroxy,hydroxymethyl, formyl, bromomethyl, vinyl, allyl, S-acetylthiomethyl,Se-acetylselenomethyl, ethynyl, 2-(trimethylsilyl)ethynyl, mercapto,mercaptomethyl, 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, anddihydroxyphosphoryl. In certain embodiments, the alkyl attachment groupcomprises a functional group selected from the group consisting ofbromo, iodo, hydroxy, formyl, vinyl, mercapto, selenyl, S-acetylthio,Se-acetylseleno, ethynyl, 2-(trimethylsilyl)ethynyl,4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, and dihydroxyphosphoryl. Incertain embodiments, the attachment group comprises an alcohol or aphosphonate. In certain preferred embodiments, the attachment group isselected from the group consisting of 4-(hydroxymethyl)phenyl,4-(S-acetylthiomethyl)phenyl, 4-(Se-acetylselenomethyl)phenyl,4-(mercaptomethyl)phenyl, 4-(hydroselenomethyl)phenyl, 4-formylphenyl,4-(bromomethyl)phenyl, 4-vinylphenyl, 4-ethynylphenyl, 4-allylphenyl,4-[2-(trimethylsilyl)ethynyl]phenyl,4-[2-(triisopropylsilyl)ethynyl]phenyl, 4-bromophenyl, 4-iodophenyl,4-hydroxyphenyl, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylbromo, iodo, hydroxymethyl, S-acetylthiomethyl, Se-acetylselenomethyl,mercaptomethyl, hydroselenomethyl, formyl, bromomethyl, chloromethyl,ethynyl, vinyl, allyl, 4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl,4-(ethynyl)biphen-4′-yl, 4-[2-(triisopropylsilyl)ethynyl]biphen-4′-yl,3,5-diethynylphenyl, and 2-bromoethyl. In certain embodiments, theheat-resistant organic molecule bearing an attachment group is selectedfrom the group consisting of5-[4-(S-acetylthiomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(mercaptomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-formylphenyl)-15-phenyl-10,20-di-p-tolylporphinatozinc(II),5-(4-bromomethylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-ethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-bromophenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-hydroxyphenyl)-10,15,20-trimesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-iodo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-iodophenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,15-bis(4-iodophenyl)-10,20-dimesitylporphinatozinc(II),5,10,15-tris(4-ethynylphenyl)-20-mesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,15-bis(4-ethynylphenyl)porphinatozinc(II),5,15-bis(3-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,10,15,20-tetrakis(4-ethynylphenyl)porphinatozinc(II),5,10-bis[4-(2-(trimethylsilyl)ethynyl)phenyl]-15,20-dimesitylporphinatozinc(II),5-(3,5-diethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),3,7-dibromo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-[4-(Se-acetylselenomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis(4-ethynylbiphen-4′-yl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5-(4-vinylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-vinylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(hydroxymethyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatocopper(II), type ctriple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphyrin],type c triple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5-[4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl]-10,15,20-tri-p-tolylporphyrin],5,10-bis[4-(2-(triisopropylsilyl)ethynyl)biphen-4′-yl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),and5,10-bis[4-(2-(triisopropylsilyl)ethynyl)phenyl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II).

In certain embodiments, the contacting comprises selectively contactingthe organic molecule to certain regions of the surface and not to otherregions. For example, the contacting can comprises selectivelycontacting the volatilized organic molecule to certain regions of thesurface and not to other regions. In certain embodiments, the contactingcomprises placing a protective coating (e.g. a making material) on thesurface in regions where the organic molecule(s) are not to be attached;contacting the molecule(s) with the surface; and removing the protectivecoating to provide regions of the surface without the organicmolecule(s). In certain embodiments, the contacting comprises contactprinting of a solution comprising the organic molecule(s) or the dryorganic molecule(s) onto the surface. In certain embodiments, thecontacting comprises spraying or dropping a solution comprising theorganic molecule(s) or applying the dry organic molecule(s) onto thesurface. In certain embodiments, the contacting comprises contacting thesurface with the molecule(s) and subsequently etching selected regionsof the surface to remove the organic molecule(s). In certainembodiments, the contacting comprises molecular beam epitaxy (MBE),and/or chemical vapor deposition (CVD), and/or plasma-assisted vapordeposition, and/or sputtering and the like. In certain embodiments, theheat-resistant organic molecule comprises a mixture at least twodifferent species of heat-resistant organic molecule and the heatingcomprises heating the mixture and/or the surface.

This invention also provides a method of coupling a redox-activemolecule (or a collection of different species of redox-activemolecules) to a surface. The method typically involves heating themolecule(s) to a gas phase; and contacting the molecule(s) to a surfacewhereby the redox-active molecule(s) couple to the surface. In certainembodiments, the redox-active molecule is covalently coupled to thesurface and/or electrically coupled to the surface. In certainembodiments, the heating is to a temperature of at least about 100° C.,preferably at least about 200° C., more preferably at least about 300°C., and most preferably at least about 400° C. Heating can beaccomplished by any convenient method, e.g. in a in a CVD device, in anMBE device, etc.

In certain embodiments, the surface can comprise a material selectedfrom the group consisting of a Group III element, a Group IV element, aGroup V element, a semiconductor comprising a Group III element, asemiconductor comprising a Group IV element, a semiconductor comprisinga Group V element, a transition metal, a transition metal oxide, andanother metal, e.g. as described above. In certain embodiments, thesurface comprises a material such as tungsten, tantalum, niobium, Au,Ag, Cu, Al, Ta, Ti, Ru, Ir, Pt, Pd, Os, Mn, Hf, Zr, V, Nb, La, Y, Gd,Sr, Ba, Cs, Cr, Co, Ni, Zn, Ga, In, Cd, Rh, Re, W, Mo, and/or oxides,nitrides, mixtures, or alloys thereof. In certain embodiments, theredox-active molecule includes, but is not limited to any of themolecules described herein. Similarly the attachment groups include, butare not limited to any of the attachment groups described herein. Incertain embodiments, the Group II, III, IV, V, or VI element, morepreferably a Group III, IV, or V, element, still more preferably a GroupIV element or a doped Group IV element (e.g., silicon, germanium, dopedsilicon, doped germanium, etc.). In certain embodiments, the contactingcomprises selectively contacting the volatilized organic molecule tocertain regions of the surface and not to other regions. In certainembodiments, the contacting comprises:placing a protective coating onthe surface in regions where the redox-active molecule is not to beattached; contacting the molecule with the surface; and removing theprotective coating to provide regions of the surface without theredox-active molecule. In certain embodiments, the contacting comprisescontacting the surface with a the molecule and subsequently etchingselected regions of the surface to remove the redox-active molecule. Incertain embodiments, the contacting comprises molecular beam epitaxy(MBE), and/or chemical vapor deposition (CVD), and/or plasma-assistedvapor deposition, and/or sputtering.

In another embodiment, this invention provides a surface of a Group II,III, IV, V, or VI element or a surface of a semiconductor comprising aGroup II, III, IV, V, or VI or a transition metal, transition metaloxide, or nitride, or alloy, or mixture having an organic moleculecoupled thereto through a covalent bond, where the organic molecule iscoupled to said surface by methods described herein. In certainembodiments, the organic molecule is a redox-active molecule andincludes, but is not limited to any of the molecules described herein.Similarly the attachment groups include, but are not limited to any ofthe attachment groups described herein. In certain embodiments, theGroup II, III, IV, V, or VI element, more preferably a Group III, IV, orV, element, still more preferably a Group IV element or a doped Group IVelement (e.g., silicon, germanium, doped silicon, doped germanium,etc.). In certain embodiments, the surface comprises a surface in atransistor and/or a surface in a memory element. In certain embodiments,the surface comprises a plurality of memory elements and/or one or moreintegrated circuit elements (e.g., a diode, a logic gate, and arectifier). In certain embodiments, the surface comprises a redox-activemolecule and the surface is is electrically coupled to a device thatreads and/or sets the oxidation state of that molecule e.g. avoltammetric device, an “amperometric device, a potentiometric device, acoulometric device, an impedance spectrometer, etc. In certainembodiments, the device comprises a sinusoidal voltammeter.

In another embodiment, this invention provides a method of fabricatingan ordered molecular assembly. The method typically involves providing aheat-resistant organic molecule (or a plurality of different heatresistant organic molecules) derivatized with an attachment group;heating the molecule and/or a surface to a temperature of at least about100° C.; where the surface comprises a Group III, IV, or V element or atransition metal or metal oxide, contacting the molecule(s) at aplurality of discrete locations on the surface whereby the attachmentgroups form covalent or ionic bonds with the surface at the plurality ofdiscrete locations. In certain embodiments, the heating is to atemperature of at least about 100° C., preferably at least about 200°C., more preferably at least about 300° C., and most preferably at leastabout 400° C. In certain embodiments, the organic molecule is aredox-active molecule and includes, but is not limited to any of themolecules described herein. Similarly the attachment groups include, butare not limited to any of the attachment groups described herein. Incertain embodiments, the Group II, III, IV, V, or VI element, morepreferably a Group III, IV, or V, element, still more preferably a GroupIV element or a doped Group IV element (e.g., silicon, germanium, dopedsilicon, doped germanium, etc.).

This invention also provide kits for coupling an organic molecule to thesurface of a type III, IV, or V material or a transition metal ortransition metal oxide. The kits typically include a containercontaining a heat-resistant organic molecule derivatized with anattachment group (e.g., as described herein) and, optionallyinstructional materials teaching coupling the organic molecule to thesurface by heating the molecule and/or the surface to a temperature ofabout 200° C. or more.

DEFINITIONS

The term “oxidation” refers to the loss of one or more electrons in anelement, compound, or chemical substituent/subunit. In an oxidationreaction, electrons are lost by atoms of the element(s) involved in thereaction. The charge on these atoms must then become more positive. Theelectrons are lost from the species undergoing oxidation and soelectrons appear as products in an oxidation reaction. An oxidation istaking place in the reaction Fe²⁺(aq)→Fe³⁺(aq)+e⁻ because electrons arelost from the species being oxidized, Fe²⁺(aq), despite the apparentproduction of electrons as “free” entities in oxidation reactions.Conversely the term reduction refers to the gain of one or moreelectrons by an element, compound, or chemical substituent/subunit.

An “oxidation state” refers to the electrically neutral state or to thestate produced by the gain or loss of electrons to an element, compound,or chemical substituent/subunit. In a preferred embodiment, the term“oxidation state” refers to states including the neutral state and anystate other than a neutral state caused by the gain or loss of electrons(reduction or oxidation).

The term “multiple oxidation states” means more than one oxidationstate. In preferred embodiments, the oxidation states may reflect thegain of electrons (reduction) or the loss of electrons (oxidation).

The terms “different and distinguishable” when referring to two or moreoxidation states means that the net charge on the entity (atom,molecule, aggregate, subunit, etc.) can exist in two different states.The states are said to be “distinguishable” when the difference betweenthe states is greater than thermal energy at room temperature (e.g., 0°C. to about 40° C.).

The term “tightly coupled” when used in reference to a subunit of amulti-subunit (e.g., polymeric) storage molecule of this inventionrefers to positioning of the subunits relative to each other such thatoxidation of one subunit alters the oxidation potential(s) of the othersubunit. In a preferred embodiment the alteration is sufficient suchthat the (non-neutral) oxidation state(s) of the second subunit aredifferent and distinguishable from the non-neutral oxidation states ofthe first subunit. In a preferred embodiment the tight coupling isachieved by a covalent bond (e.g., single, double, triple, etc.).However, in certain embodiments, the tight coupling can be through alinker, via an ionic interaction, via a hydrophobic interaction, throughcoordination of a metal, or by simple mechanical juxtaposition. It isunderstood that the subunits could be so tightly coupled that the redoxprocesses are those of a single supermolecule.

The term “electrode” refers to any medium capable of transporting charge(e.g., electrons) to and/or from a storage molecule. Preferredelectrodes are metals or conductive organic molecules. The electrodescan be manufactured to virtually any 2-dimensional or 3-dimensionalshape (e.g., discrete lines, pads, planes, spheres, cylinders, etc.).

The term “fixed electrode” is intended to reflect the fact that theelectrode is essentially stable and unmovable with respect to thestorage medium. That is, the electrode and storage medium are arrangedin an essentially fixed geometric relationship with each other. It is ofcourse recognized that the relationship alters somewhat due to expansionand contraction of the medium with thermal changes or due to changes inconformation of the molecules comprising the electrode and/or thestorage medium. Nevertheless, the overall spatial arrangement remainsessentially invariant. In a preferred embodiment this term is intendedto exclude systems in which the electrode is a movable “probe” (e.g., awriting or recording “head”, an atomic force microscope (AFM) tip, ascanning tunneling microscope (STM) tip, etc.).

The term “working electrode” is used to refer to one or more electrodesthat are used to set or read the state of a storage medium and/orstorage molecule.

The term “reference electrode” is used to refer to one or moreelectrodes that provide a reference (e.g., a particular referencevoltage) for measurements recorded from the working electrode. Inpreferred embodiments, the reference electrodes in a memory device ofthis invention are at the same potential although in some embodimentsthis need not be the case.

The term “electrically coupled” when used with reference to a storagemolecule and/or storage medium and electrode refers to an associationbetween that storage medium or molecule and the electrode such thatelectrons move from the storage medium/molecule to the electrode or fromthe electrode to the storage medium/molecule and thereby alter theoxidation state of the storage medium/molecule. Electrical coupling caninclude direct covalent linkage between the storage medium/molecule andthe electrode, indirect covalent coupling (e.g., via a linker), director indirect ionic bonding between the storage medium/molecule and theelectrode, or other bonding (e.g., hydrophobic bonding). In addition, noactual bonding may be required and the storage medium/molecule maysimply be contacted with the electrode surface. There also need notnecessarily be any contact between the electrode and the storagemedium/molecule where the electrode is sufficiently close to the storagemedium/molecule to permit electron tunneling between the medium/moleculeand the electrode.

The term “redox-active unit” or “redox-active subunit” refers to amolecule or component of a molecule that is capable of being oxidized orreduced by the application of a suitable voltage.

The term “redox-active” molecule refers to a molecule or component of amolecule that is capable of being oxidized or reduced by the applicationof a suitable voltage.

The term “subunit”, as used herein, refers to a redox-active componentof a molecule.

The term “electrochemical cell” typically refers to a referenceelectrode, a working electrode, a redox-active molecule (e.g., a storagemedium), and, if necessary, some means (e.g., a dielectric) forproviding electrical conductivity between the electrodes and/or betweenthe electrodes and the medium. In some embodiments, the dielectric is acomponent of the storage medium.

The terms “memory element”, “memory cell”, or “storage cell” refer to anelectrochemical cell that can be used for the storage of information.Preferred “storage cells” are discrete regions of storage mediumaddressed by at least one and preferably by two electrodes (e.g., aworking electrode and a reference electrode). The storage cells can beindividually addressed (e.g., a unique electrode is associated with eachmemory element) or, particularly where the oxidation states of differentmemory elements are distinguishable, multiple memory elements can beaddressed by a single electrode. The memory element can optionallyinclude a dielectric (e.g., a dielectric impregnated with counterions).

The term “storage location” refers to a discrete domain or area in whicha storage medium is disposed. When addressed with one or moreelectrodes, the storage location may form a storage cell. However if twostorage locations contain the same storage media so that they haveessentially the same oxidation states, and both storage locations arecommonly addressed, they may form one functional storage cell.

“Addressing” a particular element refers to associating (e.g.,electrically coupling) that memory element with an electrode such thatthe electrode can be used to specifically determine the oxidationstate(s) of that memory element.

The terms “read” or “interrogate” refer to the determination of theoxidation state(s) of one or more molecules (e.g., molecules comprisinga storage medium).

The phrase “output of an integrated circuit” refers to a voltage orsignal produced by a one or more integrated circuit(s) and/or one ormore components of an integrated circuit.

A “voltammetric device” is a device capable of measuring the currentproduced in an electrochemical cell as a result of the application of avoltage or change in voltage.

An “amperometric device” is a device capable of measuring the currentproduced in an electrochemical cell as a result of the application of aspecific potential field potential (“voltage”).

A “potentiometric device” is a device capable of measuring potentialacross an interface that results from a difference in the equilibriumconcentrations of redox molecules in an electrochemical cell.

A “coulometric device” is a device capable of the net charge producedduring the application of a potential field (“voltage”) to anelectrochemical cell.

An “impedance spectrometer” is a device capable of determining theoverall impedance of an electrochemical cell.

A “sinusoidal voltammeter” is a voltammetric device capable ofdetermining the frequency domain properties of an electrochemical cell.

The term “porphyrinic macrocycle” refers to a porphyrin or porphyrinderivative. Such derivatives include porphyrins with extra ringsortho-fused, or ortho-perifused, to the porphyrin nucleus, porphyrinshaving a replacement of one or more carbon atoms of the porphyrin ringby an atom of another element (skeletal replacement), derivatives havinga replacement of a nitrogen atom of the porphyrin ring by an atom ofanother element (skeletal replacement of nitrogen), derivatives havingsubstituents other than hydrogen located at the peripheral (meso-, β-)or core atoms of the porphyrin, derivatives with saturation of one ormore bonds of the porphyrin (hydroporphyrins, e.g., chlorins,bacteriochlorins, isobacteriochlorins, decahydroporphyrins, corphins,pyrrocorphins, etc.), derivatives obtained by coordination of one ormore metals to one or more porphyrin atoms (metalloporphyrins),derivatives having one or more atoms, including pyrrolic andpyrromethenyl units, inserted in the porphyrin ring (expandedporphyrins), derivatives having one or more groups removed from theporphyrin ring (contracted porphyrins, e.g., corrin, corrole) andcombinations of the foregoing derivatives (e.g., phthalocyanines,sub-phthalocyanines, and porphyrin isomers). Preferred porphyrinicmacrocycles comprise at least one 5-membered ring.

The term “porphyrin” refers to a cyclic structure typically composed offour pyrrole rings together with four nitrogen atoms and two replaceablehydrogens for which various metal atoms can readily be substituted. Atypical porphyrin is hemin.

The term “multiporphyrin array” refers to a discrete number of two ormore covalently-linked porphyrinic macrocycles. The multiporphyrinarrays can be linear, cyclic, or branched.

The terms “sandwich coordination compound” or “sandwich coordinationcomplex” refer to a compound of the formula L^(n)M^(n-1), where each Lis a heterocyclic ligand (as described below), each M is a metal, n is 2or more, most preferably 2 or 3, and each metal is positioned between apair of ligands and bonded to one or more hetero atom (and typically aplurality of hetero atoms, e.g., 2, 3, 4, 5) in each ligand (dependingupon the oxidation state of the metal). Thus sandwich coordinationcompounds are not organometallic compounds such as ferrocene, in whichthe metal is bonded to carbon atoms. The ligands in the sandwichcoordination compound are generally arranged in a stacked orientation(i.e., are generally cofacially oriented and axially aligned with oneanother, although they may or may not be rotated about that axis withrespect to one another) (see, e.g., Ng and Jiang (1997) Chemical SocietyReviews 26: 433-442). Sandwich coordination complexes include, but arenot limited to “double-decker sandwich coordination compound” and“triple-decker sandwich coordination compounds”. The synthesis and useof sandwich coordination compounds is described in detail in U.S. Pat.No. 6,212,093B1.

The term “double-decker sandwich coordination compound” refers to asandwich coordination compound as described above where n is 2, thushaving the formula L¹-M¹-L², wherein each of L¹ and L² may be the sameor different (see, e.g., Jiang et al. (1999) J. PorphyrinsPhthalocyanines 3: 322-328).

The term “triple-decker sandwich coordination compound” refers to asandwich coordination compound as described above where n is 3, thushaving the formula L¹-M¹-L²-M²-L³, wherein each of L¹, L² and L³ may bethe same or different, and M¹ and M² may be the same or different (see,e.g., Arnold et al. (1999) Chemistry Letters 483-484).

A “linker” is a molecule used to couple two different molecules, twosubunits of a molecule, or a molecule to a substrate.

A “substrate” is a, preferably solid, material suitable for theattachment of one or more molecules. Substrates can be formed ofmaterials including, but not limited to glass, plastic, silicon,germanium, minerals (e.g., quartz), semiconducting materials (e.g.,doped silicon, doped germanium, etc.), ceramics, metals, etc.

In preferred embodiments, when a metal is designated by “M” or “M^(n)”,where n is an integer, it is recognized that the metal may be associatedwith a counterion.

A “group II, III, IV, V, or VI element or material” includes the pureelement, a doped variant of the group II, III, IV, V, or VI elementand/or an oxidized variant of the group II, III, IV, V or VI element.

The term “heat-resistant organic molecule” or “heat-stable organicmolecule” refers to organic molecules (e.g., porphyrins) that are stable(e.g., show no decomposition, or substantially no decomposition) attemperature of 200° C. to 400° C., preferably at 400° C. for at least 30seconds, preferably for at least one minute, more preferably for atleast 2 to 5 minutes.

A “group III, IV, or V substrate” is a material comprising a Group III,IV, or V element.

The term “transition metals” as used herein typically refers to the 38elements in groups 3 through 12 of the periodic table. Typicallytransition metals are characterized by the fact that their valenceelectrons, or the electrons they use to combine with other elements, arepresent in more than one shell and consequently often exhibit severalcommon oxidation states. In certain embodiments, the transition metalsof this invention include, but are not limited to one or more ofscandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel,copper, zinc, yttrium, zirconium, niobium, molybdenum, technetium,ruthenium, rhodium, palladium, silver, cadmium, hafnium, tantalum,tungsten, rhenium, osmium, iridium, platinum, gold, mercury,rutherfordium, and/or oxides, and/or nitrides, and/or alloys, and/ormixtures thereof.

A “a solution comprising a heat-resistant organic molecule” is notlimited to a true solution, but also includes suspensions, dispersions,and emulsions thereof. In addition, the solution contemplates pastes,gels, aerogels, and essentially any medium suitable for “containing” theheat-resistant organic molecule(s).

A “molecule bearing an attachment group” includes molecules where theattachment group is an intrinsic component of the molecule, moleculesderivatized to add an attachment group, and molecules derivatized sothey bear a linker comprising an attachment group.

The phrase “heating a molecule” includes heating collections ofmolecules and/or increasing the kinetic energy of a single molecule.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 schematically illustrates the attachment of a heat-resistantorganic molecule to a substrate according to a method of this invention.

FIG. 2 shows illustrative heat-resistant organic molecules for use inthe methods of this invention.

FIG. 3 illustrates the optimization of concentration of porphyrinalcohol (porphyrin-OH) in THF for attachment of the porphyrin topatterned Si—H surfaces.

FIG. 4 illustrates the effect of baking time of attachment ofporphyrin-OH (compound 104) on Si—H using casting and baking process.Other conditions: 400° C., 1 mM in THF, 100 V/s.

FIG. 5 illustrates the optimization of baking temperature for attachingporphyrin alcohol (porphyrin-OH) to patterned Si—H surfaces. Otherconditions: 1 mM in THF, 60 minutes, 100 V/s.

FIG. 6A shows the cyclic voltammetric behavior of a porphyrin monolayertethered to Si(100) via a Si—O—C linkage, while FIG. 6B shows theintegrated voltammetric signal (corresponding to the charge in themonolayer) plotted as a function of the number of cycles.

FIG. 7 illustrates several basic approaches to solvent-free attachmentof organic molecules to substrates.

FIG. 8 shows the cyclic voltammetry (CyV) measurements from one of thesamples prepared as illustrated in FIG. 7, panel (a), where the sampledid not touch the molecular solution during the process.

FIG. 9 illustrates a two-zone furnace for gas phase molecularattachment.

FIG. 10 illustrates an epitaxy system utilizing a K-cell for attachmentof organic molecules to a substrate.

FIG. 11 illustrates porphyrins that have been attached via the hightemperature process described herein. Ar consists of mesityl, p-tolyl,and/or phenyl groups.

FIG. 12 shows fast-scan cyclic voltammograms (100 Vs⁻¹) of monolayers ofcompounds 6 and 8 (see FIG. 11) on p-type Si(100) microelectrodes. Thesolvent/electrolyte overlayer is composed of propylene carbonatecontaining 1.0 M Bu₄NPF₆.

DETAILED DESCRIPTION

I. Coupling an Organic Molecule to a Substrate.

This invention pertains to a novel approach to covalently attach organicmolecules to a surface of a type II, III, IV, V, or VI material, a dopedvariant thereof and/or an oxide thereof and/or to a transition metaland/or transition metal oxide or nitride. In certain embodiments (see,e.g., FIG. 1), the method involves: providing a heat-resistant organicmolecule bearing an attachment group (e.g. comprising an attachmentgroup or derivatized with an attachment group or linker bearing anattachment group); and contacting the molecule to the surface at anelevated temperature (e.g. at least about 200° C., preferably at leastabout 300° C., and more preferably at least about 400° C.). It was asurprising discovery that heat-resistant organic molecules, particularlyredox-active heat-resistant organic molecules (e.g. porphyrinicmacrocycles) will form an effective bond (e.g., a covalent bond) withthe surface under such conditions.

In addition, it was a particularly surprising discovery thatredox-active molecules so attached, remain stable and can sustainsetting and resetting of their oxidation states through many thousandsand even millions of cycles.

In various embodiments, the molecule(s) (e.g. a single species ofheat-resistant molecule or mixtures of different species ofheat-resistant molecules) can be heated and contacted to the surface,and/or the surface can be heated, and/or both the molecule(s) and thesurface can be heated. In addition the surface and/or the molecule(s)can be heated prior to contacting each other and/or while they are incontact.

In certain embodiments, the heat-resistant organic molecule is dissolvedin an organic solvent (e.g., THF, mesitylene, durene, o-dichlorobenzene,1,2,4-trichlorobenzene, 1-chloronaphthalene, 2-chloronaphthalene,N,N-dimethylformamide, N,N-dimethylacetamide, N,N-dimethylpropionamide,benzonitrile, anisole, and the like). The solvent containing themolecule can then be applied to the surface. Heating can be accomplishedby any of a variety of conventional methods. For example, the solventcan be heated before application to the surface. In certain embodiments,both the solvent and the surface can be heated before the solvent isapplied to the surface. In certain preferred embodiments, the surface isheated after application of the solvent. This is convenientlyaccomplished by baking the surface (e.g., in an oven). In certainpreferred embodiments, the surface is heated (e.g., baked) under aninert atmosphere (e.g., argon or other inert gas(es)).

In certain embodiments, particularly where large size wafers (e.g. over12 inches in diameter) are used for manufacture, solvent free methods ofthe present invention are utilized. In the solvent-free methods, SAMs ofelectro-active molecules (e.g. redox-active molecules like ferrocene andporphyrin), or other heat-resistant molecules are formed on desiredsurface (e.g. silicon, silicon dioxide, metals, metal oxides metalnitrides, etc.) without the use of any solvents. In other words, theattachment can be performed in a completely dry environment. In variousembodiments, this process converts the solid phase molecules to gasphase by heating them at appropriate temperatures and then transportingthe gas phase molecules to the desired surface. This process alsoenables separate control of the molecule and substrate temperature whichcan assist in achieving maximum attachment density. This process can beeasily applied in production since similar techniques (e.g. CVD and MBE)are already in use for depositing materials in the semiconductorindustry.

Several basic approaches to solvent-free attachment are illustrated inFIG. 7. In one approach, the heat-resistant molecule (or mixture ofmolecules) is deposited in a chamber containing the substrate (e.g. aGroup III, IV, or V element, a transition metal, a transition metaloxide or nitride, etc.). The solvent is evaporated away leaving only theheat-resistant molecule. The chamber is then heated volatilizing themolecule which then contacts and couples to the substrate surface.

In another approach illustrated in FIG. 7, the molecule is placed in thechamber as a dry powder. Again the chamber is heated volatilizing themolecule which then contacts and couples to the substrate surface.

In certain embodiments, the molecules to be coupled to the surface aredeposited directly on the surface (e.g. in a dry form or in a solventwhich is then evaporated away). The molecule and/or surface is thenheated (e.g. to 200° C. or more) and the molecule couples to the surface(e.g. via an ionic, more preferably via a covalent bond).

Various parameters can be optimized for attachment of any particularorganic molecule. These include (1) the concentration of themolecule(s), (2) the baking time, and (3) the baking temperature. FIGS.3, 4, and 5 show the results of these studies for a representativeporphyrin (molecule 104 in FIG. 2). In each figure, the left panel showsthe cyclic voltammogram of the covalently attached molecule. Thecharacteristic features of the voltammograms are indicative of covalentattachment and robust electrochemical behavior (see, e.g., Li et al.(2002 Appl. Phys. Lett. 81: 1494-1496; Roth et al. (2003) J. Am. Chem.Soc. 125: 505-517). The right panel shows the molecular coverage.Saturating coverage for this type of molecule is in the range of 10⁻¹⁰mol cm⁻². Although the three parameters above are not independent, thefigures illustrate the following key observations. First, using themethods described herein, the molecules can be attached at relativelyhigh surface coverage (in the range of 5×10⁻¹¹ mol cm⁻²) usingmicromolar concentrations of materials (see, e.g., FIG. 3). Facileattachment using extremely small amounts of material (e.g.,concentration less than about 5 mM, preferably less than about 1 mM,more preferably less than about 500 μM or 100 μM, still more preferablyless than about 10 μM, and most preferably less than about 1 μM) isdistinctly different from other procedures that have been used to anchormolecules to silicon. These procedures typically use very highconcentrations of molecules in solution or neat molecules. The use ofvery small amounts of material indicates that a few grams of informationstorage molecules could be used to make millions of chips. The use ofsmall amounts of material also indicates that relatively small amountsof organic solvents can be used, thereby minimizing environmentalhazards.

In addition, it was a surprising discovery that baking times as short asa few minutes (e.g., typically from about 1 sec to about 1 hr,preferably from about 10 sec to about 30 min, more preferably from about1 minute to about 5, 10, or 15 minutes, and most preferably from about30 sec to about 1 or 2 minutes) afford high surface coverage (FIG. 4).Short times minimize the amount of energy that is used in the processingstep.

It was also a surprising discovery that baking temperatures as high as400° C. can be used with no degradation of the molecules (FIG. 5). Thisresult is of importance in that many processing steps in fabricatingCMOS devices entail high temperature processing. In certain embodiments,preferred baking temperatures range from about 125° C. to about 400° C.,preferably from about 200° C. to about 400° C., more preferably fromabout 250° C. to about 400° C., and most preferably from about 300° C.to about 400° C.

A further significant point is that diverse functional groups on theinformation storage molecules are suitable for use in attachment tosilicon or other substrates (e.g. Group III, IV, or V elements,transition metals, transition metal oxides or nitrides, transition metalalloys, etc.). The groups include, but are not limited to, alcohol,thiol, S-acetylthiol, bromomethyl, allyl, iodoaryl, carboxaldehyde,ethyne, vinyl, hydroxymethyl. It is also noted that such groups such asethyl, methyl, or arene afforded essentially no attachment asdemonstrated by the failure to achieve substantial attachment with thezinc chelates of octaethylporphyrin, meso-tetraphenylporphyrin,meso-tetra-p-tolylporphyrin, and meso-tetramesitylporphyrin.

The successful attachment via S-acetylthiol, bromomethyl, iodoaryl,carboxaldehyde, and ethyne is unprecedented. The successful attachmentvia the iodoaryl group is extraordinarily valuable in affording a directaryl-Si attachment. The resulting information-storage molecules can bepositioned vertically from the surface, which facilitates subsequentpatterning. The ability to attach via such diverse functional groupsprovides great versatility.

While in certain embodiments, heating is accomplished by placing thesubstrate in an oven, essentially any convenient heating method can beutilized, and appropriate heating and contacting methods can beoptimized for particular (e.g., industrial) production contexts. Thus,for example, in certain embodiments, heating can be accomplished bydipping the surface in a hot solution containing the organic moleculesthat are to be attached. Local heating/patterning can be accomplishedusing for example a hot contact printer, or a laser. Heating can also beaccomplished using forced air, a convection oven, radiant heating, andthe like. The foregoing embodiments are intended to be illustrativerather than limiting.

II. The Organic Molecules.

It was a surprising discovery that a large number of organic molecules,including redox-active organic molecules, are sufficientlyheat-resistant to be amenable and even quite effective in the methods ofthis invention. Suitable heat-resistant organic molecules typicallyinclude, but are not limited to metallocenes (e.g., ferrocene),porphyrins, expanded porphyrins, contracted porphyrins, linear porphyrinpolymers, porphyrin sandwich coordination complexes, and porphyrinarrays.

Certain preferred heat-resistant organic molecules include, but are notlimited to5-[4-(S-acetylthiomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(mercaptomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-formylphenyl)-15-phenyl-10,20-di-p-tolylporphinatozinc(II),5-(4-bromomethylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-ethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-bromophenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-hydroxyphenyl)-10,15,20-trimesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-iodo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-iodophenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,15-bis(4-iodophenyl)-10,20-dimesitylporphinatozinc(II),5,10,15-tris(4-ethynylphenyl)-20-mesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,15-bis(4-ethynylphenyl)porphinatozinc(II),5,15-bis(3-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,10,15,20-tetrakis(4-ethynylphenyl)porphinatozinc(II),5,10-bis[4-(2-(trimethylsilyl)ethynyl)phenyl]-15,20-dimesitylporphinatozinc(II),5-(3,5-diethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),3,7-dibromo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-[4-(Se-acetylselenomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis(4-ethynylbiphen-4′-yl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5-(4-vinylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-vinylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(hydroxymethyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatocopper(II), type ctriple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphyrin],type c triple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5-[4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl]-10,15,20-tri-p-tolylporphyrin],5,10-bis[4-(2-(triisopropylsilyl)ethynyl)biphen-4′-yl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis[4-(2-(triisopropylsilyl)ethynyl)phenyl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),and the like.

The suitablity of particular molecules for use in the methods of thisinvention can readily be determined. The molecule(s) of interest aresimply coupled to a surface (e.g., a hydrogen passivated surface)according to the methods of this invention. Then sinusoidal voltammetrycan be performed (e.g., as described herein or in U.S. Pat. Nos.6,272,038, 6,212,093, and 6,208,553, PCT Publication WO 01/03126, or by(Roth et al. (2000) Vac. Sci. Technol. B 18: 2359-2364; Roth et al.(2003) J. Am. Chem. Soc. 125: 505-517) to evaluate 1) whether or not themolecule(s) coupled to the surface, 2) the degree of coverage(coupling); and 3) whether or not the molecule degraded during thecoupling procedure.

Table 1 illustrates the test results (electrochemical characteristics)of a number of porphyrins examined using the attachment proceduredescribed herein. For those porphyrins that attached a subjective EGFPscale was used to rate their electrochemical behavior.

TABLE 1 Electrochemical behavior of porphyrins attached to a siliconsubstrate according to the methods described herein. All substituentsare at the p-position, and each compound bears one substituent unlessnoted otherwise. cmpd # Result Structural element (non-linking units) 16 excellent ZnP—PhCH₂SAc (mesityl) 104 excellent ZnP—PhCH₂OH (mesityl)115 excellent ZnP—PhCH₂OH (p-tolyl) 132 good TD-dpe-CH₂OH 141 excellentZnP—Ph-allyl (mesityl) 153 no attachment ZnTPP 172 excellent ZnP—Ph—CHO(p-tolyl; phenyl) 178 excellent ZnP—PhCH₂Br (mesityl) 181 no attachmentZnTTP 182 no attachment ZnTMP 183 no attachment ZnOEP 184 excellentZnP—PhCCH (mesityl) 185 good ZnP—PhI (mesityl) 189 Fair ZnP—PhBr(p-tolyl) 191 excellent ZnP—PhOH (mesityl) 192 excellent (polymer)cis-ZnP—(PhCCH)₂ (mesityl) 193 Fair ZnP—Ph—B(OR)₂ (mesityl; 3,5-di-t-BuPh) 194 Fair ZnP—I (mesityl; 3,5-di-t-BuPh) 195 good cis-ZnP—(PhI)₂(mesityl) 196 excellent ZnP—PhCC-TMS (mesityl) 197 excellent (polymer)trans-ZnP—(PhCCH)₂ (mesityl) 189 good trans-ZnP—(PhI)₂ (mesityl) 199good (polymer) ZnP—(PhCCH)₃ (mesityl) 200 good trans-ZnP—(PhCCH)₂(p-t-BuPh) 201 poor trans-ZnP—(PhCCH)₂ (H) 202 good trans-ZnP-m-(PhCCH)₂(mesityl) 204 poor ZnP—(PhCCH)₄ 205 Fair TD-(PhCCH)₂ 206 excellenttrans-ZnP—(PhCC-TMS)₂ (mesityl) 207 good ZnP-Ph-3,5-(CCH)₂ (mesityl) 208poor ZnP-3,7-Br₂ (mesityl; 3,5-di-t-BuPh) 209 excellent ZnP—CC-TMS(p-tolyl) *ZnP is a zinc porphyrin. TD is a triple-decker lanthanidesandwich coordination compound (e.g., as described in U.S. Pat. No.6,212,093).It is noted that the above-described compounds are meant to beillustrative and not limiting. Other suitable compounds can readily beascertained using routine screening procedures as described herein.

It is also noted that where certain organic molecules decompose atparticular sites at high temperature (e.g., 200° C. to 400° C.) the“reactive” site can often be derivatized with a stable protecting group.The molecule can be coupled to the surface according to the methods ofthis invention and the protecting group can then be chemically removedfrom the organic molecule.

The organic molecule is typically provided in a solvent, dispersion,emulsion, paste, gel, or the like. Preferred solvents, pastes, gels,emulsions, dispersions, etc., are solvents that can be applied to theGroup II, III, IV, V, and/or VI material(s), and/or transition metalswithout substantially degrading that substrate and that solubilize orsuspend, but do not degrade the organic molecule(s) that are to becoupled to the substrate. In certain embodiments, preferred solventsinclude high boiling point solvents (e.g., solvents with an initialboiling point greater than about 130° C., preferably greater than about150° C., more preferably greater than about 180° C.). Such solventsinclude, but are not limited to benzonitrile, dimethylformamide, xylene,ortho-dichlorobenzene, and the like.

III. The Attachment Molecules.

To effect attachment to the substrate (e.g., a Group II, III, IV, V, orVI element, semiconductor, and/or oxide, and/or transition metal,transition metal oxide or nitride, etc.) the heat-resistant organicmolecule either bears one or more attachment group(s) (e.g., assubstituent(s)) and/or is derivatized so that it is attached directly orthrough a linker to one or more attachment groups.

In certain preferred embodiments, the attachment group comprises an arylor an alkyl group. Certain preferred aryl groups include a functionalgroup such as bromo, iodo, hydroxy, hydroxymethyl, formyl, bromomethyl,vinyl, allyl, S-acetylthiomethyl, Se-acetylselenomethyl, ethynyl,2-(trimethylsilyl)ethynyl, mercapto, mercaptomethyl,4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, and dihydroxyphosphoryl.Certain preferred alkyls include a functional group such as bromo, iodo,hydroxy, formyl, vinyl, mercapto, selenyl, S-acetylthio,Se-acetylseleno, ethynyl, 2-(trimethylsilyl)ethynyl,4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, and dihydroxyphosphoryl.

In certain embodiments the attachment groups include, but are notlimited to alcohols, thiols, S-acetylthiols, bromomethyls, allyls,iodoaryls, carboxaldehydes, ethynes, and the like. In certainembodiments, the attachment groups include, but are not limited to4-(hydroxymethyl)phenyl, 4-(S-acetylthiomethyl)phenyl,4-(Se-acetylselenomethyl)phenyl, 4-(mercaptomethyl)phenyl,4-(hydroselenomethyl)phenyl, 4-formylphenyl, 4-(bromomethyl)phenyl,4-vinylphenyl, 4-ethynylphenyl, 4-allylphenyl,4-[2-(trimethylsilyl)ethynyl]phenyl,4-[2-(triisopropylsilyl)ethynyl]phenyl, 4-bromophenyl, 4-iodophenyl,4-hydroxyphenyl, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylbromo, iodo, hydroxymethyl, S-acetylthiomethyl, Se-acetylselenomethyl,mercaptomethyl, hydroselenomethyl, formyl, bromomethyl, chloromethyl,ethynyl, vinyl, allyl, 4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl,4-(ethynyl)biphen-4′-yl, 4-[2-(triisopropylsilyl)ethynyl]biphen-4′-yl,3,5-diethynylphenyl, 2-bromoethyl, and the like. These attachment groupsare meant to be illustrative and not limiting.

The suitability of other attachment groups can readily be evaluated. Aheat-resistant organic molecule bearing the attachment group(s) ofinterest (directly or on a linker) is coupled to a substrate (e.g.,hydrogen-passivated silicon) according to the methods described herein.The efficacy of attachment can then be evaluated electrochemically,e.g., using sinusoidal voltammetry as described above.

The attachment groups can be substituent(s) comprising theheat-resistant organic molecule. Alternatively, the organic molecule canbe derivatized to covalently link the attachment group(s) thereto eitherdirectly or through a linker.

Means of derivatizing molecules, e.g., with alcohols or thiols are wellknown to those of skill in the art (see, e.g., Gryko et al. (1999) J.Org. Chem., 64: 8635-8647; Smith and March (2001) March's AdvancedOrganic Chemistry, John Wiley & Sons, 5th Edition, etc.).

Where the attachment group comprises an alcohol, in certain embodiments,suitable alcohols include, but are not limited to a primary alcohol, asecondary alcohol, a tertiary alcohol, a benzyl alcohol, and an arylalcohol (i.e., a phenol). Certain particularly preferred alcoholsinclude, but are not limited to 2 to 10 carbon straight chain alcohols,benzyl alcohol, and phenethyl alcohol.

When the attachment group comprises a thiol, in certain embodiments,suitable thiols include, but are not limited to a primary thiol, asecondary thiol, a tertiary thiol, a benzyl thiol, and an aryl thiol.Particularly preferred thiols include, but are not limited to 2 to 10carbon straight chain thiols, benzyl thiol, and phenethyl thiol.

IV. The Substrate.

The methods of this invention are suitable for covalently couplingorganic molecules to essentially any or all Group II, III, IV, V, or VImaterials (e.g., Group II, III, IV, V, or VI elements, semiconductors,and/or oxides thereof) and/or to transition metals, transition metaloxides, transition metal nitrides, alloys or composites comprisingtransition metals, and the like. In certain preferred embodiments, thesubstrates comprise all Group III, IV, or V materials (e.g., carbon,silicon, germanium, tin, lead), doped Group II, III, IV, V, and VIelements, or oxides of pure or doped Group II, III, IV, V, or VIelements or transition metals, transition metal oxides or transitionmetal nitrides. In certain preferred embodiments the surface is GroupIII, IV, or V material, more preferably a Group IV material (oxide,and/or doped variant), still more preferably a silicon or germaniumsurface or a doped and/or oxidized silicon or germanium surface.

It will be understood from the teachings herein that in certainembodiments, the materials that can be used for a substrate include, butare not limited to Si, Ge, SiC, Ga, Au, Ag, Cu, Al, Ta, Ti, Ru, Ir, Pt,Pd, Os, Mn, Hf, Zr, V, Nb, La, Y, Gd, Sr, Ba, Cs, Cr, Co, Ni, Zn, Ga,In, Cd, Rh, Re, W, and their oxides and nitrides.

The group II, III, IV, V, or VI element, transition metal, transitionmetal oxide or nitride can be essentially pure, or it can be doped(e.g., p- or n-doped) and/or alloyed. P- and n-dopants for use withGroup II-VI elements, in particular for use with Groups III, IV, and Velements, more particularly for use with Group IV elements (e.g.,silicon, germanium, etc.) are well known to those of skill in the art.Such dopants include, but are not limited to phosphorous compounds,boron compounds, arsenic compounds, aluminum compounds, and the like.Many doped Group II, III, IV, V, or VI elements are semiconductors andinclude, but are not limited to ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe, MgS,MgSe, MgTe, CaS, CaSe, CaTe, SrS, SrSe, SrTe, BaS, BaSe, BaTe, GaN, GaP,GaAs, GaSb, InP, InAs, InSb, AlS, AlP, AlSb, PbS, PbSe, Ge and Si andternary and quaternary mixtures thereof.

The surface can take essentially any form. For example, it can beprovided as a planar substrate, an etched substrate, a deposited domainon another substrate and the like. Particularly preferred forms includethose forms of common use in solid state electronics fabricationprocesses.

Although not necessarily required, in certain embodiments the surface iscleaned before use, e.g., using standard methods known to those of skillin the art. Thus, for example, in one preferred embodiment, the surfacecan be cleaned by sonication in a series of solvents (e.g., acetone,toluene, acetone, ethanol, and water) and then exposed to a standardwafer-cleaning solution (e.g., Piranha (sulfuric acid: 30% hydrogenperoxide, 2:1)) at an elevated temperature (e.g., 100° C.).

In certain embodiments, oxides can be removed from the substrate surfaceand the surface can be hydrogen passivated. A number of approaches tohydrogen passivation are well known to those of skill in the art. Forexample, in one approach, a flow of molecular hydrogen is passed throughdense microwave plasma across a magnetic field. The magnetic fieldserves to protect the sample surface from being bombarded by chargedparticles. Hence the crossed beam (CB) method makes it possible to avoidplasma etching and heavy ion bombardment that are so detrimental formany semiconductor devices (see, e.g., Balmashnov, et al. (1990)Semiconductor Science and Technology, 5: 242). In one particularlypreferred embodiment, passivation is by contacting the surface to bepassivated with an ammonium fluoride solution (preferably sparged ofoxygen).

Other methods of cleaning and passivating surfaces are known to those ofskill in the art (see, e.g., Choudhury (1997) The Handbook ofMicrolithography, Micromachining, and Microfabrication, Soc.Photo-Optical Instru. Engineer, Bard & Faulkner (1997) Fundamentals ofMicrofabrication, and the like).

V. Patterning the Organic Molecule(s) on the Substrate

In certain embodiments, the heat-resistant organic molecules areattached to form a uniform film across the surface of the substrate. Inother embodiments, the organic molecules are separately coupled at oneor more discrete locations on the surface. In certain embodiments,different molecules are coupled at different locations on the surface.

The location at which the molecules are coupled can be accomplished byany of a number of means. For example, in certain embodiments, thesolution(s) comprising the organic molecule(s) can be selectivelydeposited at particular locations on the surface. In certain otherembodiments, the solution can be uniformly deposited on the surface andselective domains can be heated. In certain embodiments, the organicmolecules can be coupled to the entire surface and then selectivelyetched away from certain areas.

The most common approach to selectively contacting the surface with theorganic molecule(s) involves masking the areas of the surface that areto be free of the organic molecules so that the solution or gas phasecomprising the molecule(s) cannot come in contact with those areas. Thisis readily accomplished by coating the substrate with a masking material(e.g., a polymer resist) and selectively etching the resist off of areasthat are to be coupled. Alternatively a photoactivatible resist can beapplied to the surface and selectively activated (e.g., via UV light) inareas that are to be protected. Such “photolithographic” methods arewell known in the semiconductor industry (see e.g., Van Zant (2000)Microchip Fabrication: A Practical Guide to Semiconductor Processing;Nishi and Doering (2000) Handbook of Semiconductor ManufacturingTechnology; Xiao (2000) Introduction to Semiconductor ManufacturingTechnology; Campbell (1996) The Science and Engineering ofMicroelectronic Fabrication (Oxford Series in Electrical Engineering),Oxford University Press, and the like). In addition, the resist can bepatterned on the surface simply by contact printing the resist onto thesurface.

In other approaches, the surface is uniformly contacted with themolecules. The molecules can then be selectively etched off the surfacein areas that are to be molecule free. Etching methods are well know tothose of skill in the art and include, but are not limited to plasmaetching, laser etching, acid etching, and the like.

Other approaches involve contact printing of the reagents, e.g., using acontact print head shaped to selectively deposit the reagent(s) inregions that are to be coupled, use of an inkjet apparatus (see e.g.,U.S. Pat. No. 6,221,653) to selectively deposit reagents in particularareas, use of dams to selectively confine reagents to particularregions, and the like.

In certain preferred embodiments, the coupling reaction is repeatedseveral times. After the reaction(s) are complete, uncoupled organicmolecules are washed off of the surface, e.g., using standard wash steps(e.g., benzonitrile wash followed by sonication in dry methylenechloride).

The foregoing methods are intended to be illustrative. In view of theteachings provided herein, other approaches will be evident to those ofskill in the semiconductor fabrication arts.

VI. Industrial Scale-Up.

The methods of this invention are readily scaled up for use incommercial manufacturing operations. One such scaled-up approach isillustrated in FIG. 9. This figure illustrates a two-zone furnace 1 forgas phase molecular attachment. In device, the molecule powder 2 is keptin one zone and the wafers 3 are kept in different zone. Each zone canbe individually heated (e.g. by a heater(s) 4, 5 that can beindependently regulated by a single heater control or by separate heatercontrols (6 and 7 in the illustration). Each zone can be independentlyheated to the required temperature. One can control the molecule vaporpressure by changing the temperature. This system also allows the use ofa carrier gas (e.g. Ar, N₂, etc.), fed through a gas inlet 8, throughthe oven to a gas outlet 9, which can be used to transport the moleculevapors to the wafers in other zone. This furnace can also be operated atlow pressures (sub-atmospheric) by evacuating the system with a pump atthe outlet of carrier gas. The low pressure process allows the moleculevapor pressure to be controlled very precisely. Also, it reduces theamount of impurities compared to the atmospheric process.

Another equipment configuration, illustrated FIG. 10, is suitable forhigh vacuum operation of the gas phase molecular attachment method. Inthis approach, the substrate 3 is placed in a vacuum furnace chamber 20.The molecule(s) that are to be attached are kept in an effusion cell(e.g. a knudson-cell (K-cell), for example the Low Temperature EffusionCell by Specs) 22 which is controlled by an effusion cell controller 24.By opening and closing the shutter 26 on the k-cell, one can control theamount of molecules that can reach the substrate surface and form anattached monolayer 28.

These methods are meant to be illustrative and not limiting. Using theteachings provided herein, one of skill in the art can devise numerousapproaches for heating and contacting the molecules described hereinwith a surface. Devices and methods for heating and/or volatilizing theheat-resistant molecules or mixtures of such molecules and patterning oruniformly depositing them on a surface at elevated temperature arecommercially available and well known to those of skill in the art. Suchmethods include, but are not limited to molecular beam epitaxy (MBE)(equipment available for example, from SPECS Scientific Instruments,Inc., Florida), chemical vapor deposition (CVD) (equipment available,for example, from CVD Equipment Corp.), Liquid Phase Epitaxialdeposition (LPE) (equipment available, for example, from CVD EquipmentCorp., Ronkonkoma, N.Y.), and the like.

VII. High Charge Density Materials.

It was a surprising discovery of this invention that the methodsdescribed herein, of coupling redox-active molecules to a doped orundoped substrate (e.g., a substrate comprising a group III, IV, or Velement, a transition metal, a transition metal oxide, nitride, and thelike) results in higher and more uniform packing of the organicmolecules (e.g., redox-active species) than other previously knownmethods. With redox-active organic molecules this can manifest as loweroxidative current at higher anodic potentials observed in voltametricmeasurements. In addition, a cyclic voltammogram shows sharper and moresymmetric peaks.

In addition, the improved uniformity and higher packing density ofredox-active molecules on the substrate results in materials capable ofstoring a significantly higher charge density. Thus, in preferredembodiments, this invention provides a substrate, (e.g. a group IVelement substrate) having coupled thereto one or more redox-activespecies that can store charge at a charge density of at least about 75μCoulombs/cm², preferably at least about 100 μCoulombs/cm², morepreferably at least about 150 μCoulombs/cm², and most preferably of atleast about 200 or 250 μCoulombs/cm² per non-zero oxidation state of theredox-active molecules. Such materials are useful in the fabrication ofmolecular memories (memory chips).

Where various binding moieties are used instead of redox-active species,the high uniformity and molecule density provides sensors having greatersensitivity and selectivity for a particular analyte.

VIII. Uses of Organic Molecules Coupled to a Substrate.

The methods of this invention can be used to attach essentially anyheat-resistant organic molecule to a Group II, III, IV, V, or VImaterial surface, preferably to a Group III, IV, or V surface and/or toa transition metal surface. In certain preferred embodiments, themolecule is a redox-active molecule and can be used to form a molecularmemory. In other preferred embodiments, the molecule can be essentiallyany other heat-resistant molecule. Certain other heat-resistantmolecules include, but are not limited to binding partner (e.g., certainantibodies, ligands, nucleic acids, sugars, etc.) and can be used toform a sensor for detecting particular analyte(s).

In “molecular memory” redox-active molecules (molecules having one ormore non-zero redox states) coupled to the transition metals and/orGroup II, III, IV, V, or VI materials are used to store bits (e.g., eachredox state can represent a bit). The redox-active molecule attached tothe substrate material (e.g., silicon, germanium, etc.) forms a storagecell capable of storing one or more bits in various oxidation states. Incertain embodiments, the storage cell is characterized by a fixedelectrode electrically coupled to a “storage medium” comprising one ormore redox-active molecules and having a multiplicity of different anddistinguishable oxidation states. Data is stored in the (preferablynon-neutral) oxidation states by the addition or withdrawal of one ormore electrons from said storage medium via the electrically coupledelectrode. The oxidation state of the redox-active molecule(s) can beset and/or read using electrochemical methods (e.g., cyclicvoltammetry), e.g., as described in U.S. Pat. Nos. 6,272,038, 6,212,093,and 6,208,553 and PCT Publication WO 01/03126.

Because transition metals and group II, III, IV, V, and VI materials, inparticular group IV materials (e.g., silicon, germanium, etc.), arecommonly used in electronic chip fabrication, the methods providedherein readily lend themselves to the fabrication of molecular memorychips compatible with existing processing/fabrication technologies. Inaddition, details on the construction and use of storage cellscomprising redox-active molecules can be found, in U.S. Pat. Nos.6,272,038, 6,212,093, and 6,208,553 and PCT Publication WO 01/03126.

Certain preferred redox-active molecules suitable for use in thisinvention are characterized by having a multiplicity of oxidationstates. Those oxidation states are provided by one or more redox-activeunits. A redox-active unit refers to a molecule or to a subunit of amolecule that has one or more discrete oxidation states that can be setby application of an appropriate voltage. Thus, for example, in oneembodiment, the redox-active molecule can comprise two or more (e.g., 8)different and distinguishable oxidation states. Typically, but notnecessarily, such multi-state molecules will be composed of severalredox-active units (e.g., porphyrins or ferrocenes). Each redox-activemolecule is itself at least one redox-active unit, or comprises at leastone redox-active unit, but can easily comprise two or more redox-activeunits.

Preferred redox-active molecules include, but are not limited toporphyrinic macrocycles. Particularly preferred redox-active moleculesinclude a porphyrin, an expanded porphyrin, a contracted porphyrin, aferrocene, a linear porphyrin polymer, a porphyrin sandwich coordinationcomplex, and a porphyrin array.

In certain embodiments, the redox-active molecule is a metallocene asshown in Formula I.

where L is a linker, M is a metal (e.g., Fe, Ru, Os, Co, Ni, Ti, Nb, Mn,Re, V, Cr, W), S¹ and S² are substituents independently selected fromthe group consisting of aryl, phenyl, cycloalkyl, alkyl, halogen,alkoxy, alkylthio, perfluoroalkyl, perfluoroaryl, pyridyl, cyano,thiocyanato, nitro, amino, alkylamino, acyl, sulfoxyl, sulfonyl, imido,amido, and carbamoyl. In preferred embodiments, a substituted aryl groupis attached to the porphyrin, and the substituents on the aryl group areselected from the group consisting of aryl, phenyl, cycloalkyl, alkyl,halogen, alkoxy, alkylthio, perfluoroalkyl, perfluoroaryl, pyridyl,cyano, thiocyanato, nitro, amino, alkylamino, acyl, sulfoxyl, sulfonyl,imido, amido, and carbamoyl.

Certain suitable substituents include, but are not limited to,4-chlorophenyl, 3-acetamidophenyl, 2,6-dichloro-4-trifluoromethyl, andthe like. Preferred substituents provide a redox potential range of lessthan about 2 volts. X is selected from the group consisting of asubstrate, a reactive site that can covalently couple to a substrate(e.g., an alcohol, a thiol, etc.). It will be appreciated that in someembodiments, L-X is an alcohol or a thiol. In certain instances L-X canbe replaced with another substituent (S³) like S¹ or S². In certainembodiments, L-X can be present or absent, and when present preferablyis 4-hydroxyphenyl, 4-(2-(4-hydroxyphenyl)ethynyl)phenyl,4-(hydroxymethyl)phenyl, 4-mercaptophenyl,4-(2-(4-mercaptophenyl)ethynyl)phenyl, 4-mercaptomethylphenyl,4-hydroselenophenyl, 4-(2-(4-hydroselenophenyl)ethynyl)phenyl,4-hydrotellurophenyl, 4-(hydroselenomethyl)phenyl,4-(2-(4-hydrotellurophenyl)ethynyl)phenyl, 4-(hydrotelluromethyl)phenyl,and the like.

The oxidation state of molecules of Formula I is determined by the metaland the substituents. Various suitable metallocenes are disclosed inU.S. Pat. Nos. 6,272,038, 6,212,093, and 6,208,553, and PCT PublicationWO 01/03126.

Other suitable redox-active molecules include, but are not limited toporphyrins illustrated by Formula II.

where, F is a redox-active subunit (e.g., a ferrocene, a substitutedferrocene, a metalloporphyrin, or a metallochlorin, etc.), J¹ is alinker, M is a metal (e.g., Zn, Mg, Cd, Hg, Cu, Ag, Au, Ni, Pd, Pt, Co,Rh, Ir, Mn, B, Al, Ga, Pb, and Sn), S¹ and S² are independently selectedfrom the group consisting of aryl, phenyl, cycloalkyl, alkyl, halogen,alkoxy, alkylthio, perfluoroalkyl, perfluoroaryl, pyridyl, cyano,thiocyanato, nitro, amino, alkylamino, acyl, sulfoxyl, sulfonyl, imido,amido, and carbamoyl wherein said substituents provide a redox potentialrange of less than about 2 volts, K¹, K², K³, and K⁴ are independentlyselected from the group consisting of N, O, S, Se, Te, and CH; L is alinker; X is selected from the group consisting of a substrate, areactive site that can covalently couple to a substrate. In preferredembodiments, X or L-X is an alcohol or a thiol. In some embodiments L-Xcan be eliminated and replaced with a substituent independently selectedfrom the same group as S¹ or S².

Other suitable molecules include, but are not limited to5-[4-(S-acetylthiomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(mercaptomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-formylphenyl)-15-phenyl-10,20-di-p-tolylporphinatozinc(II),5-(4-bromomethylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-ethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-bromophenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-hydroxyphenyl)-10,15,20-trimesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-iodo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-iodophenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,15-bis(4-iodophenyl)-10,20-dimesitylporphinatozinc(II),5,10,15-tris(4-ethynylphenyl)-20-mesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,15-bis(4-ethynylphenyl)porphinatozinc(II),5,15-bis(3-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,10,15,20-tetrakis(4-ethynylphenyl)porphinatozinc(II),5,10-bis[4-(2-(trimethylsilyl)ethynyl)phenyl]-15,20-dimesitylporphinatozinc(II),5-(3,5-diethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),3,7-dibromo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-[4-(Se-acetylselenomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis(4-ethynylbiphen-4′-yl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5-(4-vinylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-vinylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(hydroxymethyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatocopper(II), type ctriple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphyrin],type c triple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5-[4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl]-10,15,20-tri-p-tolylporphyrin],5,10-bis[4-(2-(triisopropylsilyl)ethynyl)biphen-4′-yl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis[4-(2-(triisopropylsilyl)ethynyl)phenyl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),and the like.

Control over the hole-storage and hole-hopping properties of theredox-active units of the redox-active molecules used in the memorydevices of this invention allows fine control over the architecture ofthe memory device.

Such control is exercised through synthetic design. The hole-storageproperties depend on the oxidation potential of the redox-active unitsor subunits that are themselves or that are used to assemble theredox-active storage media used in the devices of this invention. Thehole-storage properties and redox potential can be tuned with precisionby choice of base molecule(s), associated metals and peripheralsubstituents (Yang et al. (1999) J. Porphyrins Phthalocyanines, 3:117-147). The design of molecules for molecular memory is discussed indetail in U.S. Pat. Nos. 6,272,038, 6,212,093, and 6,208,553, and PCTPublication WO 01/03126.

IX. Kits.

In still another embodiment, this invention provides kits for practiceof the method of this invention or for use of the materials produced bymethods of this invention. In one embodiment, the kit comprises one ormore reagents used to couple an organic molecule to a type II, III, IV,V, or VI material according to the methods of this invention. Suchreagents include, but are not limited to reagents for cleaning and/orpassivating the material surface, and/or the organic molecule(s) thatare to be coupled to the surface, and/or attachment molecules forderivatizing the organic molecule(s) (e.g., reagents for derivatizing anorganic molecule with an attachment group, e.g. an alcohol, thiol,S-acetylthiol, bromomethyl, allyl, iodoaryl, carboxaldehyde, ethyne,vinyl, hydroxymethyl, etc. as described herein), and/or solvents for usein coupling the derivatized organic molecule to the surface, and/orreagents for washing the derivatized surface, and the like.

In certain embodiments, the kits comprise a type II, III, IV, V, or VImaterial having a heat-resistant organic molecule (e.g., a redox-activemolecule) coupled thereto as described herein. The type II, III, IV, V,or VI material can, in certain embodiments, comprise a molecular memoryand in, certain embodiments, comprise a sensor.

In addition, the kits can optionally include instructional materialscontaining directions (i.e., protocols) for the practice of the methodsof this invention. Preferred instructional materials provide protocolsutilizing the kit contents for coupling a heat-resistant organicmolecule to a type II, III, IV, V, or VI material according to themethods of this invention, and/or for using type II, III, IV, V, or VImaterials having coupled organic molecules as memory elements or assensors. While the instructional materials typically comprise written orprinted materials they are not limited to such. Any medium capable ofstoring such instructions and communicating them to an end user iscontemplated by this invention. Such media include, but are not limitedto electronic storage media (e.g., magnetic discs, tapes, cartridges,chips), optical media (e.g., CD ROM), and the like. Such media mayinclude addresses to internet sites that provide such instructionalmaterials.

EXAMPLES

The following examples are offered to illustrate, but not to limit theclaimed invention.

Example 1 Molecules Can Perform in Electronic Devices Under Real-WorldProcessing and Operating Conditions

The central tenet of the field of molecular electronics is thatmolecular components can be used as functional elements in place of thesemiconductor-based devices present in conventional microcircuitry (Kwokand Ellenbogen (2002) Materials Today, 28-37; Carroll and Gorman (2002)Angew. Chem. Int. Ed. 41: 4378-4400). To serve in this role, themolecular components should remain robust under daunting conditionsincluding high-temperature (e.g., 400° C.) processing steps duringmanufacture and very large numbers (10⁹-10¹²) of operational cycles overa lifetime (International Technology Roadmap for Semiconductors (ITRS),Semiconductor Industry Association, San Jose, Calif. (2000)). There hasbeen considerable skepticism whether molecular materials possessadequate stability to meet such requirements. Herein, we demonstratethat porphyrin-based information storage media meet the processing andoperating challenges required for use in computational devices.

Our approach for molecular-based information storage employsredox-active porphyrin molecules as charge-storage elements (Roth et al.(2000) Vac. Sci. Technol. B 18: 2359-2364). We have shown that thesemolecules can be covalently attached to device-grade silicon platformsto form the basis of first-generation hybrid molecular/semiconductordevices (Roth et al. (2003) J. Am. Chem. Soc. 125: 505-517). Theporphyrin-based information storage elements exhibit charge-retentiontimes that are long (minutes) compared with those of the semiconductorelements in dynamic random access memory (milliseconds) (Roth et al.(2000) Vac. Sci. Technol. B 18: 2359-2364; Roth et al. (2003) J. Am.Chem. Soc. 125: 505-517). These molecules also exhibit redoxcharacteristics that make them amenable for use as multibitinformation-storage media.

FIG. 6A shows the cyclic voltammetric behavior of a porphyrin monolayertethered to Si(100) via a Si—O—C linkage. This monolayer was formed byplacing a small amount (˜1 μL) of a dilute solution (˜100 μM) on amicron-scale photolithographically patterned, hydrogen-passivatedSi(100) platform and baking the sample at 400° C. for several minutesunder inert atmosphere conditions. The voltammetric response of theporphyrin monolayer is identical to that of porphyrin monolayers formedat much lower temperatures (100-200° C. for several hours) (Roth et al.(2003) J. Am. Chem. Soc. 125: 505-517) and demonstrates that molecularintegrity is maintained at temperatures where most organic moleculesthermally decompose. The high-temperature procedure is readily adaptableto current semiconductor fabrication technology and has the importantadded benefit that extremely small quantities of material are needed tomake a device.

The robustness of the porphyrin information-storage medium was examinedby repeatedly performing the cycle of (1) oxidizing the electricallyneutral monolayer and (2) reducing the resulting positively chargedmonolayer to its electrically neutral state. The oxidation event isequivalent to writing a bit of information; the reduction event isequivalent to erasing or destructively reading out the information. Thefive voltammograms in FIG. 6A show the response of the system after 0,2.5×10⁴, 1.8×10⁶, 1.1×10⁹, and 1.0×10¹⁰ oxidation/reduction cycles.During the experiment, the nature of the electrical cycling was varied.On some days, the system was continuously cycled for 24 hrs. On others,cycling was stopped intentionally for periods ranging from a few minutesup to 12 hrs. At one point, cycling was stopped unintentionally due toan electrical power failure. The data indicate that after an initial“burn-in” period of ˜10⁷ cycles the voltammetric response stabilizes.This robustness of the system is further illustrated in FIG. 6B whereinthe integrated voltammetric signal (corresponding to the charge in themonolayer) is plotted as a function of the number of cycles. These dataindicate that the charge-storage characteristics of the monolayerexhibit minimal variation (few percent) over the course of the entireexperiment. At the time cycling was arbitrarily stopped (>10¹⁰ cycles;˜27 days), the system showed no signs of degradation. Collectively,these data indicate that the porphyrin-based information storage mediumis extremely robust and augur well for the use of selected molecules inhybrid molecular/semiconductor electronic devices.

Example 2 Solvent Free Attachment

FIG. 7 illustrates an experimental set-up that was used to prove theconcept of gas phase molecular attachment. As illustrated in panel (a),we put a drop of molecular solution (redox-active porphyrin intetrahydrofuran, (THF) solvent) on top of a piece of silicon wafer in avial. A second piece of silicon wafer was placed next to it. We thensealed the vial and purged it with argon for several minutes toremove/dry THF. This leaves only a molecule powder on the first siliconpiece. During the purge, the argon flow was kept low so that no moleculepowder would be blown to the other silicon chip. After this step, thevials were heated at various temperatures (300-400° C. for 10-20 min).Afterwards the vials were cooled down to room temperature, and thesilicon pieces were rinsed with dichloromethane.

A second set-up is illustrated in FIG. 7 (panel b), where no solvent wasinvolved. We sealed the powder comprising the molecule together with asilicon piece in a vial, and made sure that they were not touching eachother. The vials were then purged with argon making sure that no powderwas blown over on the silicon surface. Then the vials were heated at300-400° C. for 10-20 min.

FIG. 7, panel (c) shows the third set-up used (panel c) where thesilicon substrate was kept facing the powder comprising the molecule(distance of few millimeters). The rest of the procedure was similar tothat described above.

FIG. 8 shows the cyclic voltammetry (CyV) measurements from one of thesamples prepared as illustrated in panel (a), where the sample did nottouch the molecular solution during the process. We can clearly see thepeaks associated with the redox activity of the molecule. The moleculecoverage density derived from this plot is 1×10¹³-2×10¹³ cm⁻² foroxidation and reduction peaks, which is comparable with the results fromtraditional direct liquid phase attachment process. Also, the redox peakpotentials matched our previous data.

The sample prepared according to the method illustrated in panel (b) ofFIG. 7 had electrical properties very similar to those of the sampleprepared according to the method illustrated in panel (a). Theattachment density was found to be 8×10¹³-1×10¹⁴ cm⁻² for this sample.These values are higher than those we obtained using the first approach,which may be caused by higher molecule vapor pressure in this case.

The sample produced according to the method illustrated in panel (c) ofFIG. 7 had electrical properties very similar to those of the sampleprepared according to the method illustrated in panel (b), but providehigher attachment since the spacing between the molecules and the samplewas reduced.

These experiments show that molecular attachment with high density andintegrity can be achieved by a completely “dry” process that does notrequire any solvents. We believe that this approach will be bettersuited to conventional manufacturing processes than the “wet” methods.In addition, this “dry” attachment is also compatible with large scalelow cost processing.

Example 3 Facile Covalent Attachment of Porphyrins to SemiconductorSurfaces via High Temperature Processes

The field of molecular electronics has been driven by the prospect thatdevices that rely on the bulk properties of semiconductors will fail toretain the required characteristics to function when feature sizes reachnanoscale dimensions. As a consequence, there has been much interest indeveloping molecular-based electronic materials for use in both memoryarchitectures and circuit elements (see, e.g., Kwok et al. MaterialsToday (February 2002), 28-37; Carroll and Gorman (2002) Angew. Chem.Int. Ed., 41: 4378-4400). Towards this goal, we have been engaged in aprogram aimed at constructing devices that use the properties ofmolecules to store information (Roth et al. (2000) Vac. Sci. Technol. B18: 2359-2364; Roth et al. (2003) ACS Symp. Series, 844: 51-61; Roth etal. (2003) Am. Chem. Soc., 125: 505-517; Li et al. (2002) Appl Phys.Lett., 81: 1494-1496; Li et al. (2003) Appl. Phys. Lett., 83: 198-200.).In our approach, a collection of redox-active porphyrinic moleculesattached to an electroactive surface serves as the active storagemedium, and information is stored in the discrete redox states of themolecules. The focus of our work has been developing a hybridarchitecture, where the molecular material is attached to asemiconductor platform. The implementation of hybridmolecular/semiconductor architectures as a transition technologyleverages the vast infrastructure of the semiconductor industry with theadvantages afforded by molecular-based active media.

We have shown that porphyrins (Roth et al. (2003) Am. Chem. Soc., 125:505-517) and ferrocenes (Roth et al. (2003) Am. Chem. Soc., 125:505-517; Li et al. (2002) Appl. Phys. Lett., 81: 1494-1496) can beattached to single-crystal Si platforms (and Si platforms modified withan oxide overlayer (Li et al. (2003) Appl. Phys. Lett., 83: 198-200) toform the basis of hybrid molecular/semiconductor devices. One procedurefor attaching the porphyrins to the Si platforms (eitherhydrogen-passivated or iodine-modified) involved depositing a drop of analcohol-functionalized molecule in a high-boiling solvent (e.g.,benzonitrile) onto a photolithographically patterned micron-size Sielectrode, followed by heating at ˜170° C. for several hrs, during whichtime additional solvent was added to the sample area (Roth et al. (2003)Am. Chem. Soc., 125: 505-517). Although this procedure produced highquality monolayers, the procedure is time consuming and not readilyadaptable to commercial processing at the wafer level.

The limitations of this procedure for the attachment of porphyrins to Siplatforms prompted us to explore alternative strategies. In this regard,there have been a number of recent studies exploring the attachment oforganic molecules to Si surfaces (Song and Sailor (1999) Comments onInorganic Chemistry, 21: 69-84; Bent (2002) Surf Sci., 500: 879-903;Buriak (2002) J. Chem. Rev., 102, 1271-1308). These strategies offer noadvantages (and in most cases disadvantages) for attaching porphyrins toSi. Nevertheless, the success of thermal attachment methods (both forporphyrins and other types of molecules) combined with the fact thatporphyrins are known to be stable at very high temperatures (400° C.under inert atmosphere conditions) (Miu et al. (2003) Science, 302:1543-1545) where other types of organic molecules decompose prompted usto explore very high temperature processing strategies.

In this example, we demonstrate that porphyrins containing a widevariety of aryl functional groups undergo rapid, facile attachment underhigh-temperature processing conditions. The structures of the variousmolecules successfully attached are shown in FIG. 11. The successfulattachment via bromo, iodo, bromomethyl, formyl, S-acetylthiomethylSe-acetylselenomethyl, and trimethylsilylethynyl groups isunprecedented. We further demonstrate that the high-temperatureprocessing conditions afford attachment either by direct deposition ofthe sample onto the Si substrate or sublimation onto the Si substrate.

The initial high-temperature attachment procedure involved a directdeposition approach. In this procedure, the porphyrin was firstdissolved in an organic solvent and a small drop (1 μL) of the resultingdilute solution was placed onto the micron-size silicon platform.

The 100 μm×100 μm Si platforms were prepared photolithographically fromdevice-grade wafers (B-doped Si(100); ρ=0.005-0.1 Ω cm). All materials,procedures, and techniques and instrumentation for conducting theelectrochemical studies were as described in Roth et al. (2003) Am.Chem. Soc., 125: 505-517. The surface coverage of the molecules wasdetermined by integrating the peaks in the voltammogram. The temperatureof the Si platform was measured by attaching a thermocouple directly tothe platform.

The platform was placed in a vial, which was sealed and purged with Ar.The vial was then placed on a hot plate preheated to a particulartemperature and the system was “baked” for a specified time. The Siplatform was then cooled, washed to remove non-attached porphyrin, andinterrogated voltammetrically to investigate the quality of themonolayer and determine the surface coverage as described above. FIG. 12(top panels) shows representative cyclic voltammograms of 6 and 8obtained by attaching the porphyrins using a 100 μM deposition solutionfollowed by baking at 400° C. for 2 min.

The “best” attachment conditions for direct deposition were determinedvia a systematic study that probed the effects of varying the bakingtemperature, the baking time, the concentration of the porphyrins in thedeposition solution, and the nature of the deposition solvent. The firstthree of these variables are not independent; however, the studiesrevealed the following general trends: (1) As the baking temperature isincreased, the surface coverage monotonically increases. For example,increasing the baking temperature from 100 to 400° C. (baking time 30min; deposition solution porphyrin conc. 1 mM) increased the surfaceconcentration from 1×10⁻¹¹ mol cm⁻² to ˜8×10⁻¹¹ mol cm⁻ (the saturatingcoverage for the porphyrin is ˜10⁻¹⁰ mol cm⁻²). At temperatures above400° C., no further attachment was achieved and the system degraded. (2)As the baking temperature is increased, the time required to achieve thehighest surface coverage monotonically decreases. For example, a bakingtime of 1 h was required to achieve maximum coverage at 200° C. Thistime was reduced to 2 min when the baking temperature was elevated to400° C. (3) As the concentration of the porphyrin in the depositionsolution was increased from 1 μM to 100 μM, the surface coverage for agiven baking time and temperature systematically increased. Increasingthe porphyrin concentrations above 100 μM had little effect on thecoverage. (4) Both high-boiling (benzonitrile, bp=191° C.) andlow-boiling (THF, bp=66° C.) solvents yielded essentially identicalresults for a particular set of deposition and baking conditions.

The characteristic features of the voltammograms are indicative ofcovalent attachment and robust electrochemical behavior (Roth et al.(2003) Am. Chem. Soc., 125: 505-517). Similar voltammetry was observedfor the other molecules in FIG. 11 using the same deposition conditions.Attachment also was achieved with a number of porphyrins bearing afunctional group (e.g., iodo, formyl, vinyl, ethynyl, allyl) directlyappended to the porphyrin. As controls, the zinc chelates of variousporphyrins that lack functional groups were examined. These moleculesincluded octaethylporphyrin, meso-tetraphenylporphyrin,meso-tetra-p-tolylporphyrin, and meso-tetramesitylporphyrin. Noattachment was observed for any of these porphyrins as was evident fromthe observation that the baked film was completely removed by washing(in addition, no voltammetric peaks were observed).

These results indicate that the high-temperature attachment procedure(1) has broad scope encompassing diverse functional groups, (2)tolerates a variety of arene substituents, and (3) does not affordindiscriminate attachment.

The next high-temperature attachment procedure involved an indirectdeposition approach. In this procedure, a small quantity of theporphyrin (<1 mg) was placed in the bottom of a cylindrical glasscontainer whose diameter permitted insertion into the heating vial. Thetop of the container was flat to allow the Si platform to be placed ontop with the micron-size electrode facing inward (˜3 mm above the solidsample). The vial was sealed, purged with Ar, placed on a hot platepreheated to a particular temperature, and the porphyrin was sublimedfor a specified time. The Si platform was then cooled, washed to removenon-attached porphyrin, and interrogated voltammetrically to investigatethe quality of the monolayer and determine the surface coverage.Representative cyclic voltammograms of 6 and 8 are shown in FIG. 12(bottom panels). Both of these molecules were attached by subliming at400° C. for 20 min.

The “best” attachment conditions for indirect deposition were determinedvia a systematic study that probed the effects of varying thesublimation temperature and baking time. At temperatures below 300° C.,relatively little attachment was achieved via the sublimation method. At400° C., the surface coverage monotonically increased as the sublimationtime was increased. No further coverage was observed for times longerthan 20 min.

The characteristic features of the voltammograms obtained via thesublimation method are quite similar to those obtained via the bakingmethod. Similar results were obtained for the other molecules in FIG.11.

Collectively, the studies reported herein indicate that porphyrinsbearing a variety of functional groups can be covalently attached to Sivia high-temperature processing. The method affords a nearly universalstrategy for attaching porphyrins. The baking approach is essentially“dry” inasmuch as only a small amount of solvent is used in theattachment process; the sublimation approach is totally “dry” in that nosolvents are required in the process. This latter process isparticularly appealing from a semiconductor processing perspective,wherein uniform attachment of molecules to very large (30 cm) Si wafersmight be anticipated in the manufacture of future-generation hybridmolecular/semiconductor devices.

Example 4 Attachment of Organic Molecules to Transition Metal Surfaces

Various redox molecules containing either alcohol or phosphonate tethershave been attached to sputtered W surfaces. The surfaces underwent aheat treatment in an oxidizing ambient prior to attachment. The tungstenareas were defined through photolithography. The molecule solution forattachment was prepared by dissolving molecules in benzonitrile. Thesample was kept in Ar₂ at a set temperature during the attachmentprocess. After deposition, the samples were cleaned by sonicating intetrahydrofuran. A solution of 1.0 M tetrabutylammoniumhexafluorophosphate (TBAH) (Aldrich) in propylene carbonate (PC)(Aldrich, 99.7%) was used as the supporting electrolyte. The counterelectrode was prepared by sonicating the silver wire in 7.0 M NH₄OH andrinsing it at deionized water and ethanol. The samples were measured byCyclic voltammetry and indicated excellent behavior.

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

1. A method of coupling a redox-active molecule to a surface, saidmethod comprising: heating a heat-resistant redox-active organicmolecule bearing an attachment group and/or said surface to atemperature of at least about 200° C.; and contacting said molecule tosaid surface whereby said molecule couples to said surface.
 2. Themethod of claim 1, wherein said organic molecule is electrically coupledto said surface.
 3. The method of claim 1, wherein said heating is underan inert atmosphere.
 4. The method of claim 1, wherein said heatingcomprises heating said molecule to a gas phase and said contactingcomprises contacting said gas phase to said surface.
 5. The method ofclaim 1, wherein said heating comprises heating said molecule and/orsaid surface while said molecule is in contact with said surface.
 6. Themethod of claim 1, wherein said heating comprises applying said moleculeto said surface and then simultaneously or subsequently heating themolecule and/or surface.
 7. The method of any of claims 4 through 6,wherein said molecule is not in a solvent.
 8. The method of claim 4,wherein said contacting comprises selectively contacting the volatilizedorganic molecule to certain regions of said surface and not to otherregions.
 9. The method of claim 1, wherein said heating said moleculecomprises heating said surface and/or said molecule to a temperature ofat least about 300° C.
 10. The method of claim 1, wherein said heatingsaid molecule comprises heating said surface and/or said molecule to atemperature of at least about 400° C.
 11. The method of claim 1, whereinsaid heating occurs in a CVD device.
 12. The method of claim 1, whereinsaid heating occurs in an MBE device.
 13. The method of claim 1, whereinsaid surface comprises a material selected from the group consisting ofa Group III element, a Group IV element, a Group V element, asemiconductor comprising a Group III element, a semiconductor comprisinga Group IV element, a semiconductor comprising a Group V element, atransition metal, and a transition metal oxide.
 14. The method of claim1, wherein said surface comprises a transition metal or an oxide of atransition metal selected from the group consisting of tungsten,tantalum, and niobium.
 15. The method of claim 1, wherein said surfacecomprises an element, alloy, oxide or nitride of a metal selected fromthe group consisting of Ga, Au, Ag, Cu, Al, Ta, Ti, Ru, Ir, Pt, Pd, Os,Mn, Hf, Zr, V, Nb, La, Y, Gd, Sr, Ba, Cs, Cr, Co, Ni, Zn, Ga, In, Cd,Rh, Re, W, Mo.
 16. The method of claim 13, wherein said Group III, IV,or V element is a Group IV element or a doped Group IV element.
 17. Themethod of claim 16, wherein said Group III, IV, or V element is selectedfrom the group consisting of silicon, germanium, doped silicon, anddoped germanium.
 18. The method of claim 1, wherein said surfacecomprises a hydrogen passivated surface.
 19. The method of claim 1,wherein said heat-resistant molecule is a redox-active molecule selectedfrom the group consisting of a porphyrin, a porphyrinic macrocycle, anexpanded porphyrin, a contracted porphyrin, a linear porphyrin polymer,a porphyrinic sandwich coordination complex, and a porphyrin array. 20.The method of claim 19, wherein said redox-active molecule comprises aporphyrinic macrocycle substituted at a β-position or at ameso-position.
 21. The method of claim 19, wherein said redox-activemolecule comprises a porphyrinic macrocycle containing at least twoporphyrins of equal energies held apart from each other at a spacingless than about 50 Å such that said molecule has an even or an odd holeoxidation where the hole hops between said two porphyrins, and whereinsaid odd hole oxidation state is different from and distinguishable fromanother oxidation state of said porphyrinic macrocycle.
 22. The methodof claim 1, wherein said attachment group comprises an aryl functionalgroup.
 23. The method of claim 22, wherein said aryl functional groupcomprises a functional group selected from the group consisting ofbromo, iodo, hydroxy, hydroxymethyl, formyl, bromomethyl, vinyl, allyl,S-acetylthiomethyl, Se-acetylselenomethyl, ethynyl,2-(trimethylsilyl)ethynyl, mercapto, mercaptomethyl,4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, and dihydroxyphosphoryl.24. The method of claim 1, wherein said attachment group comprises analkyl functional group.
 25. The method of claim 24, wherein said alkylattachment group comprises a functional group selected from the groupconsisting of bromo, iodo, hydroxy, formyl, vinyl, mercapto, selenyl,S-acetylthio, Se-acetylseleno, ethynyl,4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, and dihydroxyphosphoryl.26. The method of claim 1, wherein said attachment group comprises analcohol or a phosphonate.
 27. The method of claim 1, wherein saidattachment group is selected from the group consisting of4-(hydroxymethyl)phenyl, 4-(S-acetylthiomethyl)phenyl,4-(Se-acetylselenomethyl)phenyl, 4-(mercaptomethyl)phenyl,4-(hydroselenomethyl)phenyl, 4-formylphenyl, 4-(bromomethyl)phenyl,4-vinylphenyl, 4-ethynylphenyl, 4-allylphenyl,4-[2-(trimethylsilyl)ethynyl]phenyl,4-[2-(triisopropylsilyl)ethynyl]phenyl, 4-bromophenyl, 4-iodophenyl,4-hydroxyphenyl, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylbromo, iodo, hydroxymethyl, S-acetylthiomethyl, Se-acetylselenomethyl,mercaptomethyl, hydroselenomethyl, formyl, bromomethyl, chloromethyl,ethynyl, vinyl, allyl, 4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl,4-(ethynyl)biphen-4′-yl, 4-[2-(triisopropylsilyl)ethynyl]biphen-4′-yl,3,5-diethynylphenyl, and 2-bromoethyl.
 28. The method of claim 1,wherein said heat-resistant organic molecule bearing an attachment groupis selected from the group consisting of5-[4-(S-acetylthiomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(mercaptomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-[4-(hydroxymethyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-fornylphenyl)-15-phenyl-10,20-di-p-tolylporphinatozinc(II),5-(4-bromomethylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-ethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-bromophenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-hydroxyphenyl)-10,15,20-trimesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-iodo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-iodophenyl)-15,20-dimesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,15-bis(4-iodophenyl)-10,20-dimesitylporphinatozinc(II),5,10,15-tris(4-ethynylphenyl)-20-mesitylporphinatozinc(II),5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,15-bis(4-ethynylphenyl)porphinatozinc(II),5,15-bis(3-ethynylphenyl)-10,20-dimesitylporphinatozinc(II),5,10,15,20-tetrakis(4-ethynylphenyl)porphinatozinc(II),5,10-bis[4-(2-(trimethylsilyl)ethynyl)phenyl]-15,20-dimesitylporphinatozinc(II),5-(3,5-diethynylphenyl)-10,15,20-trimesitylporphinatozinc(II),3,7-dibromo-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5-[4-(2-(trimethylsilyl)ethynyl)phenyl]-10,15,20-tri-p-tolylporphinatozinc(II),5-[4-(Se-acetylselenomethyl)phenyl]-10,15,20-trimesitylporphinatozinc(II),5-(4-iodophenyl)-10,20-bis(3,5-di-tert-butylphenyl)-15-mesitylporphinatozinc(II),5,10-bis(4-ethynylphenyl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5,10-bis(4-ethynylbiphen-4′-yl)-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),5-(4-vinylphenyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-vinylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(hydroxymethyl)-10,15,20-trimesitylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatozinc(II),5-(4-allylphenyl)-10,15,20-tri-p-tolylporphinatocopper(II), type ctriple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5,15-bis(4-ethynylphenyl)-10,20-bis(4-tert-butylphenyl)porphyrin],type c triple decker[(tert-butyl)₄phthalocyaninato]Eu[(tert-butyl)₄phthalocyaninato]Eu[5-[4-[2-(4-(hydroxymethyl)phenyl)ethynyl]phenyl]-10,15,20-tri-p-tolylporphyrin],5,10-bis[4-(2-(triisopropylsilyl)ethynyl)biphen-4′-yl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II),and5,10-bis[4-(2-(triisopropylsilyl)ethynyl)phenyl]-15,20-bis(4-tert-butylphenyl)porphinatozinc(II).29. The method of claim 1, wherein said contacting comprises selectivelycontacting the organic molecule to certain regions of said surface andnot to other regions.
 30. The method of claim 29, wherein saidcontacting comprises: placing a protective coating on said surface inregions where said organic molecule is not to be attached; contactingsaid molecule with the surface; and removing the protective coating toprovide regions of the surface without said organic molecule.
 31. Themethod of claim 29, wherein said contacting comprises contact printingof a solution comprising said organic molecule or the dry organicmolecule onto said surface.
 32. The method of claim 29, wherein saidcontacting comprises spraying or dropping a solution comprising saidorganic molecule or the dry organic molecule onto said surface.
 33. Themethod of claim 29, wherein said contacting comprises contacting saidsurface with said molecule and subsequently etching selected regions ofsaid surface to remove said organic molecule.
 34. The method of claim 1,wherein said contacting comprises molecular beam epitaxy (MBE).
 35. Themethod of claim 1, wherein said contacting comprises chemical vapordeposition (CVD).
 36. The method of claim 35, wherein said contactingcomprises plasma-assisted vapor deposition.
 37. The method of claim 1,wherein said contacting comprises sputtering.
 38. The method of claim 1,wherein said molecule couples to said surface via a covalent linkage.39. The method of claim 1, wherein said surface comprises a metalselected from the group consisting of Ga, Au, Ag, Cu, Al, Ta, Ti, Ru,Ir, Pt, Pd, Os, Mn, Hf, Zr, V, Nb, La, Y, Gd, Sr, Ba, Cs, Cr, Co, Ni,Zn, Ga, In, Cd, Rh, Re, W, Mo.